Product image of Macrogol 4000 Casen Recordati (Macrogol 4000) supplied by GNH India

Macrogol 4000 Casen Recordati

Active Ingredient:
Macrogol 4000
Origin:
EU

Macrogol 4000 Casen Recordati (Macrogol 4000)

Macrogol 4000, the active ingredient in Macrogol 4000 Casen Recordati, is an osmotic laxative presented as an oral powder for solution for oral use. It is employed to relieve constipation and to prepare the bowel for diagnostic procedures in adults and children.

GNH India supplies Macrogol 4000 Casen Recordati as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Casen Recordati, S.L.

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Indications & Clinical Uses

Macrogol 4000 is used as an osmotic laxative to manage conditions affecting bowel motility and to facilitate diagnostic procedures.

  • Constipation: softens stool and promotes bowel movements in occasional and chronic constipation.
  • Bowel preparation for colonoscopy: clears the intestinal tract to improve visualization during endoscopic examinations.
  • Opioid‑induced constipation: counteracts reduced gastrointestinal motility caused by opioid therapy.
  • Chronic idiopathic constipation: provides long‑term relief for patients with persistent functional constipation.

How It Works

  • Macrogol 4000 is a high‑molecular‑weight polyethylene glycol that is poorly absorbed from the gastrointestinal tract. It retains water within the intestinal lumen by creating an osmotic gradient, increasing stool volume and softness, which stimulates peristalsis and facilitates the passage of feces without significant electrolyte shifts.

Side Effects

Macrogol 4000 may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Abdominal bloating: sensation of fullness or swelling in the abdomen.
  • Flatulence: increased intestinal gas production.
  • Nausea: mild feeling of queasiness.
  • Diarrhea: loose or watery stools.
  • Abdominal cramps: intermittent pain or discomfort.
  • Headache: mild to moderate head pain.

Serious or Rare Side Effects

  • Severe electrolyte imbalance: abnormal levels of sodium, potassium, or other electrolytes.
  • Allergic reaction: rash, itching, swelling, or difficulty breathing.
  • Severe abdominal pain: intense or persistent pain requiring medical attention.
  • Dehydration: excessive fluid loss leading to dizziness or low blood pressure.

Precautions & Warnings

When prescribing or dispensing Macrogol 4000, consider the following safety measures.

  • Assess hydration status: ensure the patient is adequately hydrated before use.
  • Renal impairment: use with caution in patients with reduced kidney function.
  • Intestinal obstruction: avoid in cases of mechanical blockage of the bowel.
  • Electrolyte monitoring: watch for signs of electrolyte disturbances during prolonged therapy.
  • Pediatric use: administer under medical supervision in children.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Macrogol 4000 can interact with other medications that affect gastrointestinal function or fluid balance.

Major Interactions (Avoid)

  • Concurrent osmotic laxatives: may cause excessive fluid loss and electrolyte imbalance.
  • Diuretics: increased risk of dehydration and electrolyte disturbances.
  • Anticholinergic agents: may reduce the laxative efficacy of macrogol.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may increase gastrointestinal irritation when combined.
  • Opioid analgesics: may counteract the laxative effect, requiring dose adjustment.
  • Certain antacids: may alter the osmotic activity of macrogol, affecting stool consistency.

Frequently Asked Questions

Macrogol 4000 Casen Recordati is an oral osmotic laxative used to relieve occasional and chronic constipation, to prepare the bowel for procedures such as colonoscopy, and to manage opioid‑induced constipation in adults and children.

The active ingredient, macrogol 4000, is a high‑molecular‑weight polyethylene glycol that remains largely unabsorbed in the gut. It draws water into the intestinal lumen, increasing stool volume and softness, which stimulates peristalsis and promotes bowel movements.

The dose of Macrogol 4000 is individualized by the prescribing healthcare professional based on the patient’s age, severity of constipation, and clinical response. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for macrogol 4000 in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Compared with stimulant laxatives, macrogol 4000 works by osmotic water retention rather than stimulating intestinal muscle activity, resulting in a gentler, more predictable effect and a lower risk of cramping. It is also preferred over saline laxatives for patients needing minimal electrolyte disturbance.

Store Macrogol 4000 at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Macrogol 4000 is supplied as an oral powder that is dissolved in water or another suitable clear liquid according to the label instructions. The solution is then taken by mouth, usually once daily or as directed by the prescriber.

Serious risks include severe electrolyte imbalance, dehydration, and rare allergic reactions such as rash, swelling, or difficulty breathing. Patients experiencing these symptoms should seek immediate medical attention.

Macrogol 4000 should be avoided in individuals with known hypersensitivity to polyethylene glycol, in patients with complete intestinal obstruction, or in those with severe renal impairment unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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